HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 15700629, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 15700626 | HCID 15700626 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15700629 | HCID 15700629 | 74.4% |
Reaction Steps
29.5 g (0.103 mol) of 3-formamido-2-(4'-chloro-phenyl) benzo(b)thiophene with 300 ml of hydrochloric acid at 25% are refluxed with stirring for 10 hours. After cooling, the mixture is poured into water, made alkaline by ammonia and extracted with CH2Cl2. By evaporating the organic phase dried over K2CO3 and recrystallising the residue in acetone, 19.9 g (73% of theory) of 3-amino-2-(4-chlorophenyl)-benzo(b)-thiophene are obtained, yellow crystals, mp. 152°-154° (benzene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04157399 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-f35a752f0dd246b1b6f7cd2fb475bd14 |
| Source note | uspto-grants-1979_06 |